← Back to catalogue

Temp-n-Toss

FDA UDI

Class II (US FDA UDI)

by American Thermal Instruments, Llc

Identity

Trade Name
Temp-n-Toss FDA UDI
Generic Name
Colour-indication patient thermometer FDA UDI
Device Name
Disposable Forehead Thermometer FDA UDI
Model / Reference
C-8735 FDA UDI
Description
Disposable Forehead Thermometer FDA UDI

Identifiers

Primary DI / UDI-DI
00029431000007 FDA UDI
FDA Product Code
KPD FDA UDI
GMDN Term
Colour-indication patient thermometer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.2200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Colour-indication patient thermometer

Temp-n-Toss by American Thermal Instruments, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Colour-indication patient thermometer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
American Thermal Instruments, Llc

Sources (1)

  • FDA UDI 16fe4d1a-aee2-439a-8fcf-fad52b4919b9 33 fields · synced May 30, 2026